567. AGERATINA LIGUSTRINA
Compositae
Nicholas Hind
Summary . Ageratina ligustrina is illustrated in colour. Its history, cultivation
and distribution are discussed and accompanied by a black and white plate of
dissections.
With a highly scented, winter fl owering, easily grown shrub de-
scribed variously as ‘ elegant ’ , ‘ everybody ’ s plant ’ , ‘ useful ’ and with
the ‘ strongest recommendation ’ one may wonder what we have all
been missing. Such have been the descriptions of the subject of
this plate, Ageratina ligustrina (DC.) R. M. King & H. Rob., off and
on since the middle of the nineteenth century, one might ask why
aren ’ t we all growing it. The species was considered good enough
to have been awarded an Award of Garden Merit in 1996 ( Royal
Horticultural Society, 2004 ), and some 30 suppliers were listed in
the RHS Plant Finder 2006 – 07 ( Lord et al., 2006 ), and an equivalent
numbers have been listed over the last fi fteen or more years (cf.
Lord, 1990, 1996 ). It is even scented enough for Genders to have
mentioned it in his encyclopaedia ( Genders, 1978 ).
Hilliers ’ Manual ( Hillier, 1977 ) suggested that the species was in-
troduced into cultivation in 1867, although Bailey (1939) hinted
that it was probably in cultivation ‘ since about 1830 under a great
variety of names, but chiefl y as E. Weinmannianum . ’ There is ample
evidence ( Körnicke, 1858; Regel, 1867; Baker, 1869; Sheppard,
1875; Dalyrymple, 1876 ; Anon., 1876; Westland, 1877; Crane,
1879 ) that there has been a lot of interest in this plant, although
relatively little has been written about it recently. It has been listed
in most of the major compendia, dictionaries and encyclopaedias
(e.g. Bean, 1973; Hillier, 1977; Thomas, 1992; Royal Horticultural
Society, 1996; Galloway, 2000 ) and was listed in one recent specialist
popular book (e.g. Sutton, 2001 ). It was certainly in cultivation at
Kew in the late 1860s.
Ageratina ligustrina belongs to the tribe Eupatorieae which contains,
amongst many other well-known plants, Ageratum conyzoides L.,
Eupatorium cannabinum L. (HEMP AGRIMONY), and Stevia rebaudiana
(Bertoni) Bertoni, the source of a natural sweetner and sugar
substitute - stevioside. Belonging to the subtribe Oxylobinae
Ageratina ligustrina DEBORAH LAMBKIN
Plate 567
R. M. King & H. Rob., with some 265 species Ageratina is the larg-
est genus and possesses perhaps two species of note, the weedy
A. adenophora (Spreng.) R. M. King & H. Rob. and A. riparia (Regel)
R. M. King & H. Rob.; King & Robinson (1987) placed A. ligustrina
in subgenus Neogreenella R. M. King & H. Rob.
The synonymy of this taxon is extremely complicated, not least by
the range of horticultural names that appear to have been applied to
it. Vatke (1872) appears to have been the fi rst author to attempt some
listing, although he has been given little, or incorrect, credit in the
literature (c.f. Voss, 1894; King & Robinson, 1987 ). Vatke ’ s list provided
twelve synonyms, and these were repeated by Voss (1894); some of
them were credited solely to Voss by King & Robinson (1987) :
‘ Eupatorium biceps Klotsch – which appeared in herb. B, as mss. and in
hort.
E. myriadenium Schauer, Linnaea 20[sic! = 19]: 721 (1847).
b weinmannianum (Regel & Koern.) based on Eupatorium weinmannianum Regel
& Koern.
Eupatorium glabellum Otto, in herb. B and in hort.
Eupatorium glabrum hort.
Eupatorium glabratum hort.
Eupatorium glaucum Huegel in hort.
Ageratum glaucum hort.
Eupatorium album hort.
Ageratum album hort.
Eupatorium odoratum hort.
Eupatorium odoratissimum hort.
Eupatorium roseum hort.
Eupatorium morisii hort., non Vis.
Eupatorium iodopappum Sch.Bip. in herb. B, in horb. hort. bot. B. ’
The only differences noted by Voss was that Ageratum album was
cited ‘ hort. non Steud. ’ , and Eupatorium b weinmannianum was com-
bined as a forma.
Other names have also appeared in horticulture including:
Eupatorium fl oribundum hort. The whole are put into context in the fol-
lowing description.
C ULTIVATION . This species has a long history of cultivation be-
ginning just after it was fi rst described and brought into cultivation
in various nurseries and botanic gardens back in the early 1800s.
Although still mentioned in the horticultural literature it has ebbed
and fl owed in favour with enthusiastic accounts on its cultivation
in the late 1800s ( Sheppard, 1875; Dalyrymple, 1876 ). Although
the plant I am growing came from stock in RBG, Kew in 1989,
the Kew plant has long-since been dead so it is clearly not persistent.
It is grown in places as far apart as the National Botanic Gardens,
Glasnevin and gardens in South Australia.
General advice has often been to over-winter the plants in cool
greenhouses, even in southern Europe ( Galloway, 2000; Sutton,
2001 ). Categories of GI, or H3 have been recorded as hardiness
ratings, suggesting that the species is tender to temperatures below
5 ̊ C (41 ̊ F)(RHS 1996). I have found it hardy to -12 ̊ C, and there
are many reports supporting this hardiness throughout the UK, and
have successfully grown the plant in my garden in Reading since
fi rst propagated from a cutting back in 1989. Several winters have
seen hard frosts, both in my front and back gardens, where it really
doesn ’ t receive much in the way of protection. The only real dam-
age, strangely, was during a sharp -6ºC frost during December of
last year (2005) when all of the developing infl orescences were killed
off. However, several open infl orescences towards the base of the
plant were unaffected.
Whether in sheltered spots, or in the cool greenhouse, this plant
certainly offers late season colour and a heady sweet scent; when
fl owering during the summer it offers much more. It is an excel-
lent plant for attracting insect, especially if it fl owers in the spring,
summer and autumn. My own plants in high summer attracted
honey bees, humble bees, bumble bees, solitary bees, hover fl ies
and butterfl ies, and provided both pollen and nectar, as well as
producing a delightful sweet scent on the hottest days, competing
extremely well with a nearby juniper and Santolina . Late autumn
and winter fl owering can add a useful burst of white when little
else is fl owering, and it seems little affected by all but the hardest
frosts. Hard frosts may affect hard-pruned plants if pruned too
early with the young shoots just starting to grow. I have both
hard-pruned plants in my garden in Reading, as well as let them
go. Early pruning, before any new growth is evident usually results
in plants fl owering the same year at about one metre tall; plants
left un-pruned can carry on fl owering and growing, often reaching
two metres tall, and almost the same across, within two or three
years. The leaves will wilt in excessive drought conditions, but
generally the plant is excellent in most soils, except the most heavy.
It enjoys full sun, but can become leggy in partial shade, which
should be avoided.
P ESTS . I have never found any serious pest problems with the
plant and even the vine weevil, which is a serious pest in gardens
in the area, leaves it well alone.
P ROPAGATION . This species is perhaps easiest to propagate by
softwood cuttings. There is some difference of opinion as to the
best time to take cuttings. Sheat (1948) recommended taking fi rm
side shoots, with heels, between October and November and placing
in a cold frame in standard compost. I prefer softwood cuttings
taken as soon as frosts have past, or even in summer (June), and
the cuttings placed in a 50:50 mix of silver sand and sphagnum
peat (or its equivalent); pots can be placed in a propagator or simply
enclosed in a large plastic bag after a thorough misting. Rooting
usually takes place in a few weeks and when well rooted the plantlets
can be potted on, or planted out into their fi nal growing positions.
By preference I let the plants establish themselves in pots so that
they can compete with surrounding plants. Too much shade or
dominating plants can check growth of young plants. Potting on
should be into John Innes No. 3 with the addition of some sharp
grit. Pot grown plants should not be allowed to dry out in hot
weather as they tend to wilt quickly. Once established, border plants
are remarkably tolerant to drought in most years.
Mansfi eld (1945) suggested that the best method of propagation
is actually by seed, which is best sown in February at between 15º
and 20ºC. Ordinary seed compost is best, although I would prefer
the addition of sharp sand or grit.
C ULTIVARS . There is only one record that I have been able to
trace for cultivars of this species: ‘ SNOWDRIFT ’ [apparently a syn-
onym of ‘ SNOWFLAKE ’ ]. This was the name applied to a cultivar
which was submitted, and given, plant breeders rights in 1992, but
withdrawn in 1994. There are no subsequent records of this cultivar,
which was apparently a ‘ whiter ’ form, and there was no detailed
description made available.
Ageratina ligustrina (DC.) R. M. King & H. Rob., Phytologia 19(4): 223
(1973).
Eupatorium ligustrinum DC., Prodr. 5: 181 (1836). Type : ‘ in Mexico ad
Tamaulipas legit cl. Berlandier .[2143] … (v.s.) ’ . Lectotype (selected here):
G-DC – the specimen clearly labelled as above; isolectotypes : G-DC,
K, US. NB. The K isolectotype has two labels, one printed blue label
(Herbarium Berlandierianum Texano-Mexicanum ’ simply with a pencilled
number on it, the other white and penned with ‘ No 2143 = 726/fl . albi
alt. 4 – 6 p./Sarahuales de Jula a Sa Barbara/Nov, 1830 ’ . It is likely that
the other collection mounted on this sheet is a further duplicate, although
labelled ‘ 2140 ’ alongside of which B.L. Robinson has commented that
‘ This “ 2140 ” is clearly a clerical error for 2143. Berlandier ’ s 2140 was a
Dyssodia . ’ The US isolectotype has only ‘ de Tula á Tampica ’ on a hand
written label, but ‘ In Mexico ad Tampico de Tamaulipas ’ on a printed
mimeographed label – of which someone has made an appropriate com-
ment.
Eupatorium micranthum Less., Linnaea 5: 138 (1830), nom. illegit., non Lag.,
Gen. Sp. Pl. : 25 (1816) = Ageratum corymbosum Zucc.
? Eupatorium semialatum Benth., Pl. Hartw. : 76 (1841). Types : [ ‘ Sequuntur
plantae Guatemalenses (N. 523 ad 570), pleraeque circa Quezaltenango
mensibus Novembri et Decembri lectae, tum in temperatis montanis, quam
in caldis urbem inter et littus Oceani Pacifi ci, perpauceae jam mense Oc-
tobri collectae circa Comitan ad fi nes Mexicanorum. ’ ] ‘ – Sunil. – Etiam in
agro Mexicano legit. cl. Graham . ’ Lectotype (selected here): Hartweg 523
– K. (See notes in discussion as to selection of lectotype, as well as dubi-
ous synonymy.) Syntype : Graham (32) – K.
E. myriadenium Schauer, Linnaea 19(6): 721 (1847). Type : ‘ In Mexico, loco
non designato: Aschenb. [ orn ] n. 358. ’ Location of type not specifi ed but
probably B ( † , presumed destroyed during WWII): isotypes may exist in
few herbaria but none located.
Eupatorium weinmannianum Regel & Körn., Index Sem. Hort. Petrop. : 41 (1857).
Type: not cited; probable isotypes K x 2.
Eupatorium biceps Klotsch ex Vatke, Bot. Zeit. 30: 719 (1872), nom. nud. pro
syn.
Eupatorium popocatapetlense Schlchtdl. ex Hemsl., Biol. Cent.-Amer., Bot. 2: 99
(1881), nom. nud.
Eupatorium ligustrinum DC. f. weinmannianum (Regel & Körn.) Voss, Vilm. Blu-
mengaert., ed. 3, 1: 448 (1894).
Eupatorium glaucum Hort. ex Sieb. & Voss, Vilm. Blumengaert., ed. 3, 1: 448
(1894), nom. nud. pro syn.
Eupatorium erythropappum B. L.Rob., Proc. Boston Soc. Nat. Hist. 31: 248 (1904).
Type : ‘ Mexico: Alvares, San Luis Potosi, 28 September to 3 October,
1902, Dr. Edw. Palmer , no. 200. ’ Holotype : GH.
Eupatorium (§ Subimbricata) caeciliae B.L.Rob., Contr. Gray Herb. 90: 23 (1930).
Type: ‘ Guatemala: mountain woods between Totonicapam and Los En-
cuentros, Departments Qeuzaltenango and Sololá, 25 Sept. 1896, Caecilie
and Eduard Seler , no. 2361. ’ Holotype : GH.
Eupatorium plethadenium Standl. & Steyerm., Publ. Field Mus. Nat. Hist. Bot.
Ser. 23: 186 (1944). Type : ‘ Guatemala: Dept. Chimaltenango: In Cupressus
forest, region of Santa Elena, Cerro de Tecpám, alt. 2,400 – 2,700 meters,
December 26, 1938, Paul C. Standley 61100. ’ Holotype : F.
Eupatorium vetularum Standl. & Steyerm., Publ. Field Mus. Nat. Hist. Bot. Ser.
23: 190 (1944). Type : ‘ Guatemala: Dept. Totonicapán: Low damp thicket,
common, region of Chiu Jolóm, mountains above Totonicapán, on the
road to Desconsuelo, alt. 2,800 – 3,100 meters, January 23, 1941, Paul C.
Standley 84404. ’ Holotype : F.
Ageratina caeciliae (B.L. Rob.) R. M. King & H. Rob., Phytologia 19(4): 220
(1970).
Ageratina plethadenia (Standl. & Steyerm.) R. M. King & H. Rob., Phytologia
24(2): 95 (1972).
Eupatorium ligustrinum DC. var. villiferum B.L. Rob., Contr. Gray Herb. n.s. 75:
10 (1925) = Ageratina saltillensis (B.L. Rob.) R. M. King & H. Rob.
D ESCRIPTION . Evergreen perennial shrub, or sometimes subshrub , to 1.5 – 2.7 ( – 5)
m tall and 2 m ( – 5m) across. Stems mid-brown, well-branched and leafy in
upper portion of older stems, or almost throughout if fl owering growth pro-
duced that year from base. Leaves opposite, petiolate, petiole 6 – 20 mm long,
grooved above, lamina 25 – 100 ( – 150) mm long x 15 – 35 ( – 45) mm wide, base
acute to acuminate or sometimes with auriculate basal portion to lamina on
petiole, discolourous, mid-green and glossy above, lighter grey-green beneath,
with very sparse (sometimes denser) adpressed eglandular hairs above and
beneath, often moderately glandular-punctate, punctae sometimes amber-
coloured, midrib prominent beneath and primary venation translucent green
and scarcely prominent beneath, midrib and primary venation insculpate
above, margins entire in lower third, coarsely and remotely serrate in upper
two thirds, apices acute. Infl orescences terminal on fl owering shoots and well-
exceeding leafy portions, corymbose, 12 – 20 cm across x 8 – 12 cm tall, branch-
lets opposite, each subtended by a much-reduced leaf-like bract. Capitula
homogamous, discoid, pedicellate, pedicels 2 – 9 mm long, terete, moderately
to densely stipitate-glandular pubescent, usually 1 – 2-bracteolate, bracteoles
scale-like, linear, c. 3 mm long x 0.3 mm wide; involucre very narrowly-
campanulate to cylindrical; phyllaries subimbricate and effectively biseriate,
lightish green at base and pinkish-green above, outer phyllaries c. 3 mm long,
glandular-punctate throughout, margins laciniate, apices long-acute, inner
phyllaries 4 – 4.5 mm long, glandular punctate throughout, margins laciniate,
apices acute to obtuse, laciniate; receptacle small, ± fl at, glabrous. Florets
(6 – ) 7 – 12, hermaphrodite, scented (often quite sweetly so), producing good
quantities of nectar, corollas actinomorphic, 5-lobed, corolla lobes c. 1 mm
long x c. 0.8 mm wide, white, mamillose inside, often sparsely glandular-
punctate outside, apices acute to obtuse, corolla tube glabrous, white, 3.5 – 4
mm long x 0.4 mm diameter at base for c. 1.5 mm widening in upper part
to c. 1 mm; anther cylinder partially exserted, pinkish to pinkish-purple,
anther collar slightly thicker than fi lament and often very pale brown, fi la-
ments connected to corolla tube above narrower basal tube, glabrous, apical
anther appendage pinkish to whitish, broadly lanceolate, apices obtuse, basal
anther appendage shortly tailed, pinkish, entire, acute; style base glabrous
and somewhat swollen but not into distinct node, style shaft glabrous, style
arms c. 2.5 mm long, at fi rst erect, becoming ascending and fi nally spreading,
papillate in 2 lateral bands. Achenes 2.5 mm long, prismatic, body and ribs
concolorous, body blackish, sparsely glandular-punctate throughout and with
sparse twin-hairs on ribs, twin-hairs with unequal acute apices and scarcely
separated; carpopodium pale, cylindrical and appearing constricted above at
base of achene; pappus setae 2 – 3.5 mm long, barbellate, at fi rst a very subtle
pink turning pale brown with age, persistent and often somewhat fragile.
Fig. 1.
D ISTRIBUTION . Mexico, Guatemala, El Salvador, Costa Rica. However,
Mansfi eld (1945) and Genders (1978) gave the origin of the species, as E.
micranthum , as Chile, and Chile and Mexico, respectively. Baker (1869) sug-
gested ‘ A native of South America, the exact country not known. ’ and Anon
(1876) ‘ … a native of Brazil ’ for E. weinmannianum . All of them were clearly
in error!
H ABITAT . 900 – 2600 m. Montane cloud forest ( Turner 1997 ).
E TYMOLOGY . The specifi c epithet was clearly given by de Candolle because
of the plant ’ s leaves resembling those of Ligustrum spp.
F LOWERING T IME . Pruned plants may fl ower between August and November
or December, but the species can fl ower from March to May, July to September,
etc., and may well fl ower at least three times a year.
C YTOLOGY . n = 51 univalents ( Turner 1997 ).
U SES . Other than as a valuable horticultural plant, this species has no
documented uses, unless E. semialatum is included within its synonymy; this is
discussed further below.
V ERNACULAR N AMES . I NCENSE B USH , W EINMANN ’ S E UPATORIUM . One slightly
wayward internet site even referred to it just as ‘ Hemp Agrimony ’ simply
because it was listed under Eupatorium ; PRIVET-LEAVED HEMP AGRIMONY might
have been more appropriate.
D ISCUSSION . On a purely taxonomic point, it is worth comment-
ing upon the inclusion of E. semialatum in the synonymy of Ageratina
ligustrina , and the typifi cation of the former name. Bentham ’ s ac-
count of Hartweg ’ s collections (Bentham (1841) is sometimes mis-
interpreted by authors. Whilst his account is primarily based on
Hartweg ’ s collections, Bentham did include a number of other col-
lections in his account when he declared that they were the same
as Hartweg ’ s; this is especially true of Graham ’ s. The description
of Eupatorium semialatum is one such description which, although
based on Hartweg 532, actually cited an unnumbered Mexican Gra-
ham collection at the end of the protologue. Williams ’ comments
( Williams 1976 ) suggest that Hartweg 532 is the ‘ type ’ , although there
is no indication that he was aware of the Graham material. I do not
accept this as lectotypifi cation. The Hartweg 532 collection in K is
apparently from ‘ Sunil ’ ; the Graham collection (mounted with Hart-
weg 532 – ex Herb. Benthamianum) in K is numbered ‘ 32 ’ on the
sheet, since the collection has no label. I have selected Hartweg 523
specimen in K as the lectotype (see above).
© The Board of Trustees of the Royal Botanic Gardens, Kew 2006. 285
Fig. 1. Ageratina ligustrina . A, fl owering capitulum; B, l.s. capitulum; C, fl oret; D, corolla,
opened out showing attachment point of anther fi laments; E, anther; F, style base; G, style arm; H,
achene; J, detail showing twin hair from achene; L, detail showing apical portion of pappus seta.
Scale bars: A-H = 1 mm. Drawn by Margaret Tebbs from live material cultivated by the author in
Reading.
I have included E. semialatum with an element of doubt in the
synonymy of Ageratina ligustrina . Robinson (1926), King & Robinson
(1987) and Turner (1997) were of the opinion that E. semialatum
was a synonym of A. ligustrina . However, Williams (1976) expressed
some doubt, recognizing two separate species, and this is to some
degree supported by Lang (2001) and Lang et al. (2002) , following
detailed phytochemical work on sesquiterpene lactones extracted
from the leaves of both taxa. Lang et al. ’ s contention ( Lang et al.,
2002 ) was that antiplasmodially active sesquiterpene lactones (eudes-
manolides), present in E. semialatum have not yet been found in
A. ligustrina . In Central America leaves of the plant named as
E. semialatum have been used against malaria and dysentery, as well
as against other diseases and clearly the presence or absence of
these chemicals in the more widespread A. ligustrina is of some in-
terest. Apparent absence of chemicals in plant extracts is always
contentious and may simply indicate exceptionally low, or trace,
amounts. Whether this is enough to separate the two species will
need further, more detailed, morphological investigations.
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